scholarly journals Intracranial dermoid cyst rupture with midbrain and thalamic infarction

Neurology ◽  
2009 ◽  
Vol 72 (8) ◽  
pp. 769-769 ◽  
Author(s):  
M. G. Kang ◽  
K. J. Kim ◽  
J. I. Seok ◽  
D. K. Lee
2021 ◽  
Vol 2 (24) ◽  

BACKGROUND Intracranial deposits of fat droplets are an unusual presentation of a spinal dermoid cyst after spontaneous rupture and are even more uncommon after trauma. Here, the authors present a case with this rare clinical presentation, along with a systematic review of the literature to guide decision making in these patients. OBSERVATIONS A 54-year-old woman with Lynch syndrome presented with severe headache and sacrococcygeal pain after a traumatic fall. Computed tomography of the head revealed multifocal intraventricular and intracisternal fat deposits, which were confirmed by magnetic resonance imaging (MRI) of the neuroaxis; in addition, a ruptured multiloculated cyst was identified within the sacral canal with proteinaceous/hemorrhagic debris, most consistent with a sacral dermoid cyst with rupture into the cerebrospinal fluid (CSF) space. An unruptured sacral cyst was later noted on numerous previous MRI scans. In our systematic review, we identified 20 similar cases, most of which favored surgical treatment. LESSONS Rupture of an intraspinal dermoid cyst must be considered when intracranial fat deposits are found in the context of cauda equina syndrome, meningism, or hydrocephalus. Complete tumor removal with close postoperative follow-up is recommended to decrease the risk of complications. CSF diversion must be prioritized if life-threatening hydrocephalus is present.


Neurology ◽  
2006 ◽  
Vol 66 (12) ◽  
pp. 1937-1937 ◽  
Author(s):  
G. Plans ◽  
A. Aparicio ◽  
C. Majos
Keyword(s):  

2015 ◽  
Vol 25 (4) ◽  
pp. 461-464
Author(s):  
Can Yaldiz ◽  
Yusuf K. Duransoy ◽  
Mesut Mete ◽  
Tamay Şimsek ◽  
Aydin İşisağ ◽  
...  

2020 ◽  
Vol 59 (20) ◽  
pp. 2583-2586
Author(s):  
Makoto Takahashi ◽  
Madoka Tanabe ◽  
Akira Inaba ◽  
Satoshi Orimo

2018 ◽  
Vol 110 (4) ◽  
pp. e428
Author(s):  
C. Fortin ◽  
C. Hur ◽  
T. Falcone

2019 ◽  
pp. 60-62
Author(s):  
Diallo AC ◽  
Tendeng JN ◽  
Ndong A ◽  
Diao ML ◽  
Thiam O ◽  
...  

Background: Ovarian dermoid cyst is a benign congenital tumor. It is often incidentally diagnosed and can be revealed in very rare cases by spontaneous rupture. We report the case of a ruptured ovarian dermal cyst complicated by generalized peritonitis. Case report: This was a 20-year-old female patient, who consulted for abdominal pain associated with fever and vomiting. Physical examination found generalized abdominal contracture. Plain abdominal radiography found pneumoperitoneum. Biology showed leukocytosis at 18000 / mm3. Median laparotomy revealed a collection 2000 cc of pus with a ruptured right ovarian mass. An adnexectomy with lavage of abdominal cavity were performed. Anatomopathological examination concluded to an ovarian dermoid cyst with no sign of malignancy. The postoperative course was uneventful. Conclusion: Rupture of a dermoid cyst of the ovary is a rare acute complication. Examination of the operative specimen is mandatory to eliminate malignancy. Keywords: Ovary; Dermoid cyst; Rupture; Acute complication; Peritonitis; Ovary


2011 ◽  
Vol 93 (5) ◽  
pp. e39-e40 ◽  
Author(s):  
SJ Fossey ◽  
JNL Simson

This case report documents the presentation and management of a 26-year-old female patient diagnosed with SEP secondary to dermoid cyst rupture. The authors postulate that acute chemical peritonitis secondary to dermoid cyst rupture can develop into SEP resulting in the clinical features depicted in this case report.


2017 ◽  
Vol 2017 (9) ◽  
Author(s):  
Elias Antoniades ◽  
Marios Themistocleous ◽  
Evangelos Drosos ◽  
Dimitrios Giakoumettis ◽  
Kyriakos Paraskeva ◽  
...  
Keyword(s):  

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